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Cystathionine gamma-lyase expression Is regulated by exogenous hydrogen peroxide in the mammalian cells.

机译:胱硫醚γ-裂解酶的表达受哺乳动物细胞中外源性过氧化氢的调节。

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Hydrogen sulfide (H2S), as an endogenous signaling molecule in mammals, shows a variety of biological effects. Cystathionine gamma-lyase (CSE)/H2S pathway has been implicated in scavenging reactive oxygen species (ROS) in the mammalian cells. Therefore, we first investigated the regulatory effects of exogenously applied hydrogen peroxide (H2O2) on CSE expression in the mammalian cells. African green monkey kidney fibroblastlike cells (COS-7 cells) or human embryonic kidney 293 cells (HEK 293 cells) were transfected with CSE promoter-luciferase reporter constructs and treated with H2O2 of 1, 5, and 10 microM for 0.5 and 1.5 h at 37 degrees C. The transfected cells were assayed for firefly luciferase activities normalized by Renilla luciferase activity. Human lung adenocarcinoma cells (A549 cells) or human liver cancer cells (SMMC-7721 cells) were treated with H2O2 of 1, 5, and 10 microM for 0.5 and 1.5 h at 37 degrees C, and were then harvested and analyzed by Western blotting and quantitative RT-PCR. Our results showed that the treatment of a medium concentration (5 microM) of H2O2 at a longer time (1.5 h) upregulated CSE expression in the mammalian cells at the levels of the promoter, message RNA, and protein. Collectively, exogenously applied H2O2 can not only markedly affect CSE mRNA and protein expression, but also can affect the CSE promoter activity in the mammalian cells. Our observations indicate that that exogenous H2O2 can upregulate the expression of the CSE gene in the mammalian cells, which will provide the possibility of the scavenging effect of the CSE gene indirectly on ROS in the mammalian cells. However, the regulatory mechanism involved in the effects of exogenously applied H2O2 on CSE expression in the mammalian cells need be further studied.
机译:硫化氢(H2S)作为哺乳动物的一种内源性信号分子,显示出多种生物学效应。胱硫醚γ-裂解酶(CSE)/ H2S途径与清除哺乳动物细胞中的活性氧(ROS)有关。因此,我们首先研究了外源施加的过氧化氢(H2O2)对哺乳动物细胞中CSE表达的调节作用。将非洲绿猴肾成纤维细胞样细胞(COS-7细胞)或人胚肾293细胞(HEK 293细胞)转染CSE启动子-荧光素酶报告基因构建体,并在1,5和10 microM的H2O2中于0.5和1.5 h进行处理。 37℃。测定转染的细胞的萤火虫荧光素酶活性,该活性通过海肾荧光素酶活性标准化。将人肺腺癌细胞(A549细胞)或人肝癌细胞(SMMC-7721细胞)在37摄氏度下分别用1、5和10 microM的H2O2处理0.5和1.5 h,然后收集并通过Western blot分析和定量RT-PCR。我们的结果表明,在更长的时间(1.5小时)中处理中等浓度的H2O2(5 microM),可在哺乳动物细胞中以启动子,信息RNA和蛋白质水平上调CSE表达。总的来说,外源施加的H2O2不仅可以显着影响CSE mRNA和蛋白质表达,而且还可以影响哺乳动物细胞中CSE启动子的活性。我们的观察结果表明,外源性H2O2可以上调CSE基因在哺乳动物细胞中的表达,这将为CSE基因间接清除哺乳动物细胞中ROS的可能性提供可能性。然而,涉及外源施加的H2O2对哺乳动物细胞中CSE表达的影响的调节机制需要进一步研究。

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